Loxhd1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Loxhd1
lipoxygenase homology domains 1
MGI:1914609

8 phenotypes from 3 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Loxhd1^mpc188H/Loxhd1^mpc188H involves: BALB/c * C3H/HeH * C57BL/6J	deafness	J:234901
Loxhd1^mpc231H/Loxhd1^mpc231H involves: BALB/c * C3H/HeH * C57BL/6J	deafness	J:234901
Loxhd1^sba/Loxhd1^sba involves: C57BL/6J	abnormal auditory brainstem response	J:154318
	abnormal cochlear hair cell morphology	J:154318
	absent distortion product otoacoustic emissions	J:154318
	cochlear ganglion degeneration	J:154318
	cochlear hair cell degeneration	J:154318
	decreased startle reflex	J:119820
	increased or absent threshold for auditory brainstem response	J:119820

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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